Persistence of Protection Against Hepatitis B Virus Infection Among Adolescents Vaccinated With Recombinant Hepatitis B Vaccine Beginning at Birth: A 15-Year Follow-Up Study

BACKGROUND:Long-term follow-up studies of populations that received recombinant hepatitis B (HB) vaccination beginning at birth are limited. METHODS:Micronesian adolescents who had received 3 doses of recombinant HB vaccine (Recombivax 5 μg at birth, 2.5 μg at 2 months, 2.5 μg at 6 months) and teste...

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Veröffentlicht in:The Pediatric infectious disease journal 2008-10, Vol.27 (10), p.881-885
Hauptverfasser: Bialek, Stephanie R, Bower, William A, Novak, Ryan, Helgenberger, Louisa, Auerbach, Steven B, Williams, Ian T, Bell, Beth P
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container_end_page 885
container_issue 10
container_start_page 881
container_title The Pediatric infectious disease journal
container_volume 27
creator Bialek, Stephanie R
Bower, William A
Novak, Ryan
Helgenberger, Louisa
Auerbach, Steven B
Williams, Ian T
Bell, Beth P
description BACKGROUND:Long-term follow-up studies of populations that received recombinant hepatitis B (HB) vaccination beginning at birth are limited. METHODS:Micronesian adolescents who had received 3 doses of recombinant HB vaccine (Recombivax 5 μg at birth, 2.5 μg at 2 months, 2.5 μg at 6 months) and tested negative for antibody to HB core antigen (anti-HBc) 2 years after primary vaccination (baseline testing) were followed up 15 years after primary vaccination. After testing for anti-HBc, HB surface antigen (HBsAg), and antibody to HBsAg (anti-HBs), participants received a booster dose of HB vaccine. An anamnestic response was defined as an increase in anti-HBs concentrations to a level ≥10 mIU/mL 14 days postbooster. RESULTS:Of the 105 participants, 42 (40.0%) had anti-HBs concentrations ≥10 mIU/mL on baseline testing. At 15 years, 8 (7.6%) were anti-HBc positive; none were HBsAg positive. Of the remaining 97, 7 (7.3%) had anti-HBs concentrations ≥10 mIU/mL. Of the 96 who received a booster dose, 46 (47.9%) had an anamnestic response; final antibody concentrations were 10-99 mIU/mL for 17 (17.7%) and >100 mIU/mL for 29 (30.2%). Participants with anti-HBs concentrations ≥10 mIU/mL on baseline testing were more likely to have an anamnestic response at 15 years [26/39 (66.7%) versus 20/57 (35.1%); P = 0.003]. CONCLUSIONS:Fifteen years after primary vaccination starting at birth, 8% of participants had evidence of past HB virus infection, but none had chronic infection. Absence of an anamnestic response to an additional vaccine dose, seen in half of participants, might indicate waning immunity.
doi_str_mv 10.1097/INF.0b013e31817702ba
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METHODS:Micronesian adolescents who had received 3 doses of recombinant HB vaccine (Recombivax 5 μg at birth, 2.5 μg at 2 months, 2.5 μg at 6 months) and tested negative for antibody to HB core antigen (anti-HBc) 2 years after primary vaccination (baseline testing) were followed up 15 years after primary vaccination. After testing for anti-HBc, HB surface antigen (HBsAg), and antibody to HBsAg (anti-HBs), participants received a booster dose of HB vaccine. An anamnestic response was defined as an increase in anti-HBs concentrations to a level ≥10 mIU/mL 14 days postbooster. RESULTS:Of the 105 participants, 42 (40.0%) had anti-HBs concentrations ≥10 mIU/mL on baseline testing. At 15 years, 8 (7.6%) were anti-HBc positive; none were HBsAg positive. Of the remaining 97, 7 (7.3%) had anti-HBs concentrations ≥10 mIU/mL. Of the 96 who received a booster dose, 46 (47.9%) had an anamnestic response; final antibody concentrations were 10-99 mIU/mL for 17 (17.7%) and &gt;100 mIU/mL for 29 (30.2%). Participants with anti-HBs concentrations ≥10 mIU/mL on baseline testing were more likely to have an anamnestic response at 15 years [26/39 (66.7%) versus 20/57 (35.1%); P = 0.003]. CONCLUSIONS:Fifteen years after primary vaccination starting at birth, 8% of participants had evidence of past HB virus infection, but none had chronic infection. Absence of an anamnestic response to an additional vaccine dose, seen in half of participants, might indicate waning immunity.</description><identifier>ISSN: 0891-3668</identifier><identifier>EISSN: 1532-0987</identifier><identifier>DOI: 10.1097/INF.0b013e31817702ba</identifier><identifier>PMID: 18756185</identifier><identifier>CODEN: PIDJEV</identifier><language>eng</language><publisher>Baltimore, MD: Lippincott Williams &amp; Wilkins, Inc</publisher><subject>Adolescent ; Biological and medical sciences ; Female ; Follow-Up Studies ; Hepatitis B - immunology ; Hepatitis B - prevention &amp; control ; Hepatitis B Antibodies - blood ; Hepatitis B Antibodies - immunology ; Hepatitis B Core Antigens - blood ; Hepatitis B Core Antigens - immunology ; Hepatitis B Surface Antigens - blood ; Hepatitis B Surface Antigens - immunology ; Hepatitis B Vaccines - administration &amp; dosage ; Hepatitis B Vaccines - immunology ; Human viral diseases ; Humans ; Immunization Schedule ; Immunization, Secondary ; Immunologic Memory ; Infant ; Infectious diseases ; Male ; Medical sciences ; Vaccines, Synthetic - administration &amp; dosage ; Vaccines, Synthetic - immunology ; Viral diseases ; Viral hepatitis</subject><ispartof>The Pediatric infectious disease journal, 2008-10, Vol.27 (10), p.881-885</ispartof><rights>2008 Lippincott Williams &amp; Wilkins, Inc.</rights><rights>2008 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c2445-14f5a47560dfcb3c7acc14e22277e39a9f77c0260417814a9b31cb1dafa555753</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=20691641$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18756185$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bialek, Stephanie R</creatorcontrib><creatorcontrib>Bower, William A</creatorcontrib><creatorcontrib>Novak, Ryan</creatorcontrib><creatorcontrib>Helgenberger, Louisa</creatorcontrib><creatorcontrib>Auerbach, Steven B</creatorcontrib><creatorcontrib>Williams, Ian T</creatorcontrib><creatorcontrib>Bell, Beth P</creatorcontrib><title>Persistence of Protection Against Hepatitis B Virus Infection Among Adolescents Vaccinated With Recombinant Hepatitis B Vaccine Beginning at Birth: A 15-Year Follow-Up Study</title><title>The Pediatric infectious disease journal</title><addtitle>Pediatr Infect Dis J</addtitle><description>BACKGROUND:Long-term follow-up studies of populations that received recombinant hepatitis B (HB) vaccination beginning at birth are limited. METHODS:Micronesian adolescents who had received 3 doses of recombinant HB vaccine (Recombivax 5 μg at birth, 2.5 μg at 2 months, 2.5 μg at 6 months) and tested negative for antibody to HB core antigen (anti-HBc) 2 years after primary vaccination (baseline testing) were followed up 15 years after primary vaccination. After testing for anti-HBc, HB surface antigen (HBsAg), and antibody to HBsAg (anti-HBs), participants received a booster dose of HB vaccine. An anamnestic response was defined as an increase in anti-HBs concentrations to a level ≥10 mIU/mL 14 days postbooster. RESULTS:Of the 105 participants, 42 (40.0%) had anti-HBs concentrations ≥10 mIU/mL on baseline testing. At 15 years, 8 (7.6%) were anti-HBc positive; none were HBsAg positive. Of the remaining 97, 7 (7.3%) had anti-HBs concentrations ≥10 mIU/mL. Of the 96 who received a booster dose, 46 (47.9%) had an anamnestic response; final antibody concentrations were 10-99 mIU/mL for 17 (17.7%) and &gt;100 mIU/mL for 29 (30.2%). Participants with anti-HBs concentrations ≥10 mIU/mL on baseline testing were more likely to have an anamnestic response at 15 years [26/39 (66.7%) versus 20/57 (35.1%); P = 0.003]. CONCLUSIONS:Fifteen years after primary vaccination starting at birth, 8% of participants had evidence of past HB virus infection, but none had chronic infection. Absence of an anamnestic response to an additional vaccine dose, seen in half of participants, might indicate waning immunity.</description><subject>Adolescent</subject><subject>Biological and medical sciences</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Hepatitis B - immunology</subject><subject>Hepatitis B - prevention &amp; control</subject><subject>Hepatitis B Antibodies - blood</subject><subject>Hepatitis B Antibodies - immunology</subject><subject>Hepatitis B Core Antigens - blood</subject><subject>Hepatitis B Core Antigens - immunology</subject><subject>Hepatitis B Surface Antigens - blood</subject><subject>Hepatitis B Surface Antigens - immunology</subject><subject>Hepatitis B Vaccines - administration &amp; dosage</subject><subject>Hepatitis B Vaccines - immunology</subject><subject>Human viral diseases</subject><subject>Humans</subject><subject>Immunization Schedule</subject><subject>Immunization, Secondary</subject><subject>Immunologic Memory</subject><subject>Infant</subject><subject>Infectious diseases</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Vaccines, Synthetic - administration &amp; 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control</topic><topic>Hepatitis B Antibodies - blood</topic><topic>Hepatitis B Antibodies - immunology</topic><topic>Hepatitis B Core Antigens - blood</topic><topic>Hepatitis B Core Antigens - immunology</topic><topic>Hepatitis B Surface Antigens - blood</topic><topic>Hepatitis B Surface Antigens - immunology</topic><topic>Hepatitis B Vaccines - administration &amp; dosage</topic><topic>Hepatitis B Vaccines - immunology</topic><topic>Human viral diseases</topic><topic>Humans</topic><topic>Immunization Schedule</topic><topic>Immunization, Secondary</topic><topic>Immunologic Memory</topic><topic>Infant</topic><topic>Infectious diseases</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Vaccines, Synthetic - administration &amp; dosage</topic><topic>Vaccines, Synthetic - immunology</topic><topic>Viral diseases</topic><topic>Viral hepatitis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bialek, Stephanie R</creatorcontrib><creatorcontrib>Bower, William A</creatorcontrib><creatorcontrib>Novak, Ryan</creatorcontrib><creatorcontrib>Helgenberger, Louisa</creatorcontrib><creatorcontrib>Auerbach, Steven B</creatorcontrib><creatorcontrib>Williams, Ian T</creatorcontrib><creatorcontrib>Bell, Beth P</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The Pediatric infectious disease journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bialek, Stephanie R</au><au>Bower, William A</au><au>Novak, Ryan</au><au>Helgenberger, Louisa</au><au>Auerbach, Steven B</au><au>Williams, Ian T</au><au>Bell, Beth P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Persistence of Protection Against Hepatitis B Virus Infection Among Adolescents Vaccinated With Recombinant Hepatitis B Vaccine Beginning at Birth: A 15-Year Follow-Up Study</atitle><jtitle>The Pediatric infectious disease journal</jtitle><addtitle>Pediatr Infect Dis J</addtitle><date>2008-10</date><risdate>2008</risdate><volume>27</volume><issue>10</issue><spage>881</spage><epage>885</epage><pages>881-885</pages><issn>0891-3668</issn><eissn>1532-0987</eissn><coden>PIDJEV</coden><abstract>BACKGROUND:Long-term follow-up studies of populations that received recombinant hepatitis B (HB) vaccination beginning at birth are limited. METHODS:Micronesian adolescents who had received 3 doses of recombinant HB vaccine (Recombivax 5 μg at birth, 2.5 μg at 2 months, 2.5 μg at 6 months) and tested negative for antibody to HB core antigen (anti-HBc) 2 years after primary vaccination (baseline testing) were followed up 15 years after primary vaccination. After testing for anti-HBc, HB surface antigen (HBsAg), and antibody to HBsAg (anti-HBs), participants received a booster dose of HB vaccine. An anamnestic response was defined as an increase in anti-HBs concentrations to a level ≥10 mIU/mL 14 days postbooster. RESULTS:Of the 105 participants, 42 (40.0%) had anti-HBs concentrations ≥10 mIU/mL on baseline testing. At 15 years, 8 (7.6%) were anti-HBc positive; none were HBsAg positive. Of the remaining 97, 7 (7.3%) had anti-HBs concentrations ≥10 mIU/mL. Of the 96 who received a booster dose, 46 (47.9%) had an anamnestic response; final antibody concentrations were 10-99 mIU/mL for 17 (17.7%) and &gt;100 mIU/mL for 29 (30.2%). Participants with anti-HBs concentrations ≥10 mIU/mL on baseline testing were more likely to have an anamnestic response at 15 years [26/39 (66.7%) versus 20/57 (35.1%); P = 0.003]. CONCLUSIONS:Fifteen years after primary vaccination starting at birth, 8% of participants had evidence of past HB virus infection, but none had chronic infection. Absence of an anamnestic response to an additional vaccine dose, seen in half of participants, might indicate waning immunity.</abstract><cop>Baltimore, MD</cop><cop>Philadelphia, PA</cop><cop>Hagerstown, MD</cop><pub>Lippincott Williams &amp; Wilkins, Inc</pub><pmid>18756185</pmid><doi>10.1097/INF.0b013e31817702ba</doi><tpages>5</tpages></addata></record>
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subjects Adolescent
Biological and medical sciences
Female
Follow-Up Studies
Hepatitis B - immunology
Hepatitis B - prevention & control
Hepatitis B Antibodies - blood
Hepatitis B Antibodies - immunology
Hepatitis B Core Antigens - blood
Hepatitis B Core Antigens - immunology
Hepatitis B Surface Antigens - blood
Hepatitis B Surface Antigens - immunology
Hepatitis B Vaccines - administration & dosage
Hepatitis B Vaccines - immunology
Human viral diseases
Humans
Immunization Schedule
Immunization, Secondary
Immunologic Memory
Infant
Infectious diseases
Male
Medical sciences
Vaccines, Synthetic - administration & dosage
Vaccines, Synthetic - immunology
Viral diseases
Viral hepatitis
title Persistence of Protection Against Hepatitis B Virus Infection Among Adolescents Vaccinated With Recombinant Hepatitis B Vaccine Beginning at Birth: A 15-Year Follow-Up Study
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